ID   Ws-HMG
AC   CVCL_U700
SY   WS-HMG
DR   ATCC; CRL-1253
DR   Wikidata; Q54994418
RX   PubMed=4083156;
CC   Discontinued: ATCC; CRL-1253; true.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C3447; Werner syndrome
DI   ORDO; Orphanet_902; Werner syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 8
//
RX   PubMed=4083156; DOI=10.1007/978-1-4684-7853-2_17;
RA   Tanaka, Kiyoji
RA   Yamamura, Ken-ichi
RA   Fukuchi, Kenichiro
RA   Kawai, Kazuhiko
RA   Kumahara, Yuichi
RT   "Cell fusion studies in the Werner syndrome.";
RL   Adv. Exp. Med. Biol. 190:341-351(1985).
//